SRPK2, SRSF protein kinase 2, 6733

N. diseases: 51; N. variants: 11
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6466055
rs6466055 		1.000 0.040 7 105288617 intron variant A/C snv 0.60
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 3 2014 2019
dbSNP: rs2057884
rs2057884 		1.000 0.040 7 105289803 intron variant T/C snv 0.59
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 2 2017 2019
dbSNP: rs1142
rs1142 		0.851 0.040 7 105115879 intron variant C/T snv 0.31
CUI: C0271084
Disease: Exudative age-related macular degeneration
Exudative age-related macular degeneration 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1142
rs1142 		0.851 0.040 7 105115879 intron variant C/T snv 0.31
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1142
rs1142 		0.851 0.040 7 105115879 intron variant C/T snv 0.31
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1142
rs1142 		0.851 0.040 7 105115879 intron variant C/T snv 0.31
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs1142
rs1142 		0.851 0.040 7 105115879 intron variant C/T snv 0.31
CUI: C2237660
Disease: exudative macular degeneration
exudative macular degeneration 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1142
rs1142 		0.851 0.040 7 105115879 intron variant C/T snv 0.31
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1144
rs1144 		7 105115908 intron variant T/C snv 0.31
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2018 2018
dbSNP: rs1144
rs1144 		7 105115908 intron variant T/C snv 0.31
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs2057884
rs2057884 		1.000 0.040 7 105289803 intron variant T/C snv 0.59
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs41563
rs41563 		1.000 0.040 7 105212207 intron variant G/A;C snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs41563
rs41563 		1.000 0.040 7 105212207 intron variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs4580973
rs4580973 		1.000 0.040 7 105263212 intron variant A/G snv 0.45
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs4580973
rs4580973 		1.000 0.040 7 105263212 intron variant A/G snv 0.45
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs4730073
rs4730073 		7 105215424 intron variant C/A;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs55658584
rs55658584 		7 105354274 intron variant G/A snv 0.19
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs6968355
rs6968355 		1.000 0.040 7 105117803 3 prime UTR variant T/C snv 0.18 0.14
CUI: C0154778
Disease: Myopia, Degenerative
Myopia, Degenerative 		Eye Diseases 0.700 1.000 1 2012 2012
dbSNP: rs7787448
rs7787448 		7 105156888 intron variant T/A snv 0.84
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs7789569
rs7789569 		1.000 0.040 7 105287139 intron variant T/C snv 0.59
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2018 2018